Canonical Allele Identifier: CA1618747831
Gene: HLA-E HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30490205C= , CM000668.2:g.30490205C= GRCh38
NC_000006.11:g.30457982C= , CM000668.1:g.30457982C= GRCh37
NC_000006.10:g.30565961C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376630.5:c.335-35C= MANE Select ENSP00000365817.4:n.335-35C=
ENST00000376630.4:c.335-35C= ENSP00000365817.4:n.335-35C=
ENST00000484194.1:n.566C=
ENST00000493699.1:n.485-35C=
NM_005516.5:c.335-35C= NP_005507.3:n.335-35C=
XM_017010807.1:c.458-35C= XP_016866296.1:n.458-35C=
XM_017010808.1:c.458-35C= XP_016866297.1:n.458-35C=
XM_017010809.2:c.335-35C= XP_016866298.1:n.335-35C=
NM_005516.6:c.335-35C= MANE Select NP_005507.3:n.335-35C=
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